基于条形码的空间转录组学的深度图像先验生成超分辨率图像。

IF 4.3 Q1 BIOCHEMICAL RESEARCH METHODS Cell Reports Methods Pub Date : 2025-01-27 Epub Date: 2024-12-26 DOI:10.1016/j.crmeth.2024.100937
Jeongbin Park, Seungho Cook, Dongjoo Lee, Jinyeong Choi, Seongjin Yoo, Sungwoo Bae, Hyung-Jun Im, Daeseung Lee, Hongyoon Choi
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引用次数: 0

摘要

空间分辨转录组学(ST)提供了一种分析基因原位表达的强大工具,彻底改变了生物学领域。然而,目前的ST方法,特别是基于条形码的方法,在从稀疏分布在幻灯片中的条形码重建高分辨率图像方面存在局限性。在这里,我们提出了SuperST,一种能够从低分辨率ST库重建密集矩阵(高分辨率和非零膨胀矩阵)的算法。SuperST基于深度图像先验,将空间基因表达模式重构为图像矩阵。与以前的方法相比,SuperST生成的输出图像更接近于给定基因表达图谱的免疫荧光图像。此外,我们还演示了如何将SuperST创建的图像与计算机视觉算法相结合。在此背景下,我们提出了一种从图像中提取特征的方法,该方法有助于基因的空间聚类。通过为每个基因提供密集的原位基质,SuperST可以成功解决分辨率和零膨胀问题。
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Generation of super-resolution images from barcode-based spatial transcriptomics by deep image prior.

Spatially resolved transcriptomics (ST) has revolutionized the field of biology by providing a powerful tool for analyzing gene expression in situ. However, current ST methods, particularly barcode-based methods, have limitations in reconstructing high-resolution images from barcodes sparsely distributed in slides. Here, we present SuperST, an algorithm that enables the reconstruction of dense matrices (higher-resolution and non-zero-inflated matrices) from low-resolution ST libraries. SuperST is based on deep image prior, which reconstructs spatial gene expression patterns as image matrices. Compared with previous methods, SuperST generated output images that more closely resembled immunofluorescence images for given gene expression maps. Furthermore, we demonstrated how one can combine images created by SuperST with computer vision algorithms. In this context, we proposed a method for extracting features from the images, which can aid in spatial clustering of genes. By providing a dense matrix for each gene in situ, SuperST can successfully address the resolution and zero-inflation issue.

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来源期刊
Cell Reports Methods
Cell Reports Methods Chemistry (General), Biochemistry, Genetics and Molecular Biology (General), Immunology and Microbiology (General)
CiteScore
3.80
自引率
0.00%
发文量
0
审稿时长
111 days
期刊最新文献
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